Low energy fuse and method of manufacture

ABSTRACT

A low energy fuse is extruded as a single ply primary tube 1 from a plastic resin blend with particulate energetic material 2 being internally distributed in a manner known per se, said resin blend comprising a major amount of an orientable polymer, for example, linear low density polyethylene to provide structural integrity and a minor amount of a modifier to impart enhanced particle retentive properties to the tube and preferably also containing a polymer or copolymer to impart melt strength and aid in tube extrusion.

This is a division of application No. 07/581,411, filed Sep. 12, 1990now abandoned which is a continuation of application Ser. No.07/306,013, filed Feb. 3, 1989 now abandoned.

The present invention relates to an improved, low energy fuse for use incommercial blasting, improved materials useful in its manufacture and toa method for producing such a fuse.

The use of non-electric explosives initiation systems is now well knownin the blasting art. Generally, these systems comprise the use of one ormore lengths of detonating fuse cord each having attached at one endthereof an instantaneous or delay blasting cap. When the opposite end ofthe cord is initiated by means of an explosive initiator, such as a capor priming trunk line fuse cord, the detonating fuse is detonated and anexplosive wave is transmitted along its length at high velocity to setoff the attached blasting cap. The use of such a system is generallychosen where there may be hazards involved in using an electricinitiation system and electric blasting caps.

In the past, many improvements have been made in the quality andreliability of non-electric initiation systems and in detonating fusecord. An early but significant development was disclosed in our Britishpatent No 808 087 (equals U.S. Pat. No. 2,993,236). This provided asolution to the problem of how to safely incorporate an explosive corein a thermoplastic tubular sheath during extrusion. The techniquedisclosed therein can be widely applied to production of tubularproducts for use in initiation systems. One such product is shown inBritish Patent No. 1 238 503 (equals U.S. Pat. No. 3,590,739; CA 878056) which discloses a detonating fuse which comprises a tube havingonly a thin layer of a reactive substance coated on the inner areathereof rather than a core. Such a fuse is marketed under the registeredtrade mark "NONEL". Commonly, this type of fuse has come to be known asa shock wave conductor and will be referred to as such hereinafter.

The production of shock wave conductors of small diameter has beenrestricted to use of a limited number of polymers due to the principalproperties sought for the product. The product development trend in theart to meet such problems has been to provide laminated plastics tubescomprising an inner and outer layer of differing plastics to satisfyrequirements of reactive substance adhesion and mechanical strengthrespectively. A shock wave conductor in the form of a two-ply laminatedtube, the outer ply of which provides reinforcement and resistsmechanical damage, is disclosed in GB 2 027 176 (U.S. Pat. No.4,328,753; CA 1 149 229). Likewise in U.S. Pat. No. 4,607,573, a methodis described for the manufacture of a two-ply or multiply shock tubewherein the outer covering is applied only after the inner tube has beenstretched to provide the desired core load per unit length. Furtherexamples of such over coated tubes are disclosed in U.S. Pat. No.4,757,764 which proposes use of the tubes of the type disclosed in theabove-mentioned U.S. Pat. No. 4,607,573 with non-self-explosive reactivematerial within the tube. Other disclosures of the use ofnon-self-explosive reactive material are to be found in Brazilian PatentNo. PI 8104552, CA 878 056, GB 2 152 643 and U.S. Pat. Nos. 4,660,474and 4,756,250.

While the invention of the shock wave conductor has been an importantcontribution to the art of blasting, the known shock wave conductors arenot without disadvantages. Since the reactive substance within the tubeonly comprises a thin surface coating which adheres to, but is not boundto the tube, then only certain special plastics have in practice beenfound suitable to provide the necessary adhesion. Such special plasticstend to be both expensive and to lack mechanical strength. Whenprotected by an outer layer of material, as disclosed in U.S. Pat. Nos.4,328,753 and 4,607,573, the mechanical properties are improved.

SUMMARY OF THE INVENTION

A need has arisen, therefore, for a shock wave conductor which retainsall the explosive properties of the tubes currently in use and which isalso possessed of great mechanical and tensile strength but at lowproduction cost.

According to the present invention, a low energy shock wave conductor isprovided which comprises an extruded single-wall, dimensionally stableplastic tube having an inner surface coated with a particulate reactiveenergetic material, the plastic of the said tube comprising asubstantially homogeneous blend of a major amount of a draw orientablepolymer resin lacking adequate reactive material-retaining properties,and a minor amount of a modifier which is a miscible or compatiblematerial which imparts an enhanced reactive material-retainingcapability to the said extruded plastic tube.

Most favourable results are achieved in most instances when the polymeris substantially orientated linearly and this is best achieved by colddrawing the tube after melt consolidation. As used herein the term "colddrawing" means irreversible extension with a localised draw point of theextruded tube at any stage after the polymer has left the extruder andcooled sufficiently to consolidate a permanent tubular structure butremains plastic or sufficiently so to permit stretching under appliedstress to thereby orientate the crystallites in the direction of tubelength. Thus cold drawing may be carried out at any stage after the tubehas taken shape after extrusion and has begun to cool from its extrusiontemperature. Therefore it should be noted that the temperature of "colddrawing" lies suitably in the range of from about ambient roomtemperature to about 180° C. or higher depending on the polymer(s)chosen and it will be recognised that the temperature profile of thecold drawing stage(s) need not be uniform so that the post-extrusiontemperature treatment of the tube may be variable. Additionally,intermediate or terminal relaxation stages may be employed, as are wellknown in the synthetic fibre art, to "stress relieve" the cold drawntube and thereby impart improved dimensional stability to the tube. Itis envisaged that normally artificial cooling of the extruded tube willbe applied such as forced air and/or water cooling to control thetemperature during post extrusion treatment. The resulting tube is safeto handle and is easily reeled for storage or transport. Of course thefinished tube may be treated externally with agents to improveresistance to water and oil, especially diesel, permeability. Ordinarilya thin film or coating will suffice. Alternatively, the polymer blendmay include a further resin to improve oil resistance. The tube can beovercoated with another layer of polymer as in the prior art tubes butthere is no perceived advantage in doing so.

Tests, including microscopic examination, carried out on the improvedtubes made so far in accordance with the invention indicate that thedraw-orientable polymer resin is in the form of a continous matrixwhilst said compatible material is mostly present within the matrix asdiscrete noncontiguous particles, sized about 0.5 μ, or fibrils a fewmicrons in length, with aspect ratios typically of from about 6 up toabout 10 oriented along the tube axis. The structural state of saidmiscible material is less certain because inherently there are no clearphase boundaries to be highlighted by electron microscopy. However wehave noted that those miscible polymeric materials that impart goodparticle adhesion properties at the inner tube surface appear to bepresent to a substantial extent as indistinctly segregated zones of moreconcentrated material. Thus electron microscopy (viewing regions up to20 μ across) reveals arbitrary random microstructure in the plasticmatrix consistent with such zoning. It has further been observed that inmany instances the miscible or compatible material is, following meltextrusion, distributed such that it has a greater concentration at theinner surface of the tube than in the body of the matrix which providesoptimum exposure to interaction with the reactive material and favorableperformance in the resulting shock wave conductor. The distribution ofthe miscible or compatible material will vary depending on the physicaland chemical properties of the selected material.

The polymer tube components may be pro-blended in a suitable mixer priorto supply to the melt extrusion equipment to ensure proper mixing ofmaterial with the matrix polymer. The observed surface enrichment uponmelt extrusion is a surprising effect and provides a surface presence ofthe desired powder adherent material substantially larger than thepopulation of components in the tube material would imply. Thisphenomenon is believed to be achievable by a number of mechanisms, or ahelpful combination of such mechanisms, depending on the particularpolymer matrix and powder adherent materials present. Presently favouredexplanations are first preferential wetting or coating of the extrusiondie surfaces by the dispersed material in the molten polymer matrix, andsecond migration of material under shear gradients in the extrusion headto the die head surface, i.e. rheological causes. The evidence of innersurface enrichment both in the as-extruded tube and that following colddrawing is scientifically demonstrable by use of well known physicaltechniques such as ESCA.

DETAILED DESCRIPTION OF INVENTION

The miscible or compatible material is preferably a miscible orcompatible polymer or copolymer resin or a lower molecular weightmaterial of like properties capable of improving reactivematerial-retaining properties of the matrix polymer by one or more ofthe following mechanisms; (i) chemical interaction such as ionic orhydrogen bonding; (ii) physical interaction such as polar attraction,tack or surface-wetting and (iii) electrostatic interaction with theselected reactive material. In fact virtually any material which can besuccessfully introduced to the bulk matrix-forming polymer and survivethe extrusion process without degenerating or disrupting the formationof the tube can be used provided it has the capability to impart thedesired improvement in reactive material-retaining property to thematrix polymer. Suitable materials can be recognised by theircompatibility with the selected bulk resin and by having pendant or freefunctional groups which will interact with the chosen reactive materialby e.g. polar attraction, hydrogen bonding, ionic attraction withoutnecessarily forming an ionic bond. Alternatively the molecular structureis such that interaction is by physical attributes such as tack, highsurface energy or surface conditions e.g. roughness which could bemodified by inclusion of ultrafine fillers such as silica at levels ofperhaps 0.5-1.0%.

The bulk polymer matrix of which the tube is mainly composed broadlycomprises olefinic polymers, including ethylene/alpha-olefin copolymerswhere the olefin monomer may have from 4 to 16 carbon atoms such as1-butene, 1-hexene, 1-octene, 4-methyl-1-pentene etc. These typicallyhave a melt flow index of from 0.1 to 2 and a density of from 900 to 950kg.m⁻³. In general suitable matrix polymers will be fibre formingpolymers. Advantages of these polymers are their ease of processing inextrusion equipment, structural strength and generally lower cost thancurrent shock tube components.

The plastic preferably also comprises a minor amount of a polymer orcopolymer resin or cross-linking agent which is miscibie in the saidmatrix polymer resin and which imparts melt strength and aids in tubeextrusion. Such a material may be an ethylene/acrylic acid estercopolymer or a copolymer of ethylene and vinyl acetate. The acrylicesters are preferably lower alkyl esters such as methyl or butylacrylates.

Thus a suitable tube comprises a blend of 60 to 97% by weight of apolyolefin resin, e.g. linear low density polyethylene, (optionallyincluding from 5 to 45% weight of a second resin which is apolyolefin-miscible or compatible polymer, copolymer or cross-linkingagent which imparts melt strength to the blend and aids in tubeextrusion) and from 2 to 25%, preferably up to 10%, by weight of a thirdpolyolefin-miscible or compatible resin which is a surface propertymodifying polymer or copolymer such as an ethylene/acrylic acid ormethacrylic acid copolymer which may be wholly or partially neutralizede.g. an ionomer such as Surlyn 1855 (Trade Mark for a Du Pont product).

A linear low density polyethylene which may constitute up to about 97%of the polymer blend and which is used in a preferred embodiment of thetube of the invention desirably has a melt flow index (MFI) of around1.0. The polyethylene-miscible or compatible resin which imparts meltstrength to the polymer blend can advantageously be, for example,ethylene/vinyl acetate copolymer or a low density polyethylene having amelt index of 3 or less. The polyethylene-miscible or compatiblepowder-retention enhancing resin may be any acidic or ionomeric-basedco-polymer such as, for example, PRIMACOR, an ethylene-acrylic acidcopolymer, sold by Dow Chemical Company.

The method of the invention comprises the steps of extruding a melt ofthe blended constituents of the plastic tube through a wide annular diein the form of a thick walled tube while distributing particulatereactive energetic material in a core load per unit length on the innerwall of said thick walled tube and elongating the said thick walled tubeto form a localized drawing point by cold drawing, to increase the tubetensile strength, to reduce the said wall thickness and to reduce thecore load per unit length of the said reactive material. The manner ofextruding the thick walled tube whilst introducing the core load ofreactive material is similar to that disclosed in GB 808 087 (U.S. Pat.No. 2,993,236) and is widely understood by those in this art. The sizesfor shock tube are virtually standardized throughout the art atapproximately 3 mm O.D. and 1 mm I.D. by the need for compatibility withexisting detonators etc. Thus it will be apparent to those skilled inthe art that sizing dies, where required, amount of melt drawing andcold drawing will be selected to provide an equivalent or differentsized product. It may be suitable to start from extrusion of a primarytube of about 6 to 10 mm O.D. and about 3 mm I.D. Significant drawingbelow tube consolidation temperatures may be most appropriate. Howeverin view of the diversity of compositions now discovered to be useful forproducing such tubes it is not considered that definite ranges can bespecified for drawing. However a natural draw ratio of at least 4:1,weight for weight of equal lengths of undrawn against drawn tube, may bemost favorable which is perhaps equivalent to a mechanical draw ratio ofabout 5 to 8:1 Therefore, due consideration must be had to the type ofmatrix polymer chosen and any necessary minor operating adjustmentsascertained by brief preliminary trial or experimentation. Guidelinesfor same may be determined from the non-limitative Examples hereinaftergiven.

The plastic tube shock wave conductor is preferably manufactured in sucha manner as to provide a tensile strength of up to 170 newtons persquare millimetre. An effective minimum coreload for high velocity shocktubes would be about 15 mg.m⁻¹ but loadings of reactive material of upto 20 mg.m⁻¹ are possible, or even higher as indicated in theabove-mentioned specifications e.g. 25 to 60 mg per linear meter asindicated in U.S. Pat. No. 4,757,764. Tube dimensions are a matter ofchoice and would be affected by the required internal diameter and theneed to obtain a self-supporting tube but normally these would be from2.5 to 3.3 mm O.D. and about 1.3 mm I.D.

Suitable materials for use as the draw orientable matrix polymer includelinear polyethylenes such as those currently commercially availableunder the Trade Marks "Aecithene", particularly LF 3020, LF 3081 and LF3100; "Dowellex", especially 2045-A, 2049 and 2075; Du Pont 12J1; Esso3121.73; Idemitsu polyethylene-L 0134H; Mitsubishi polyethylene-LL H20E,F30F and F30H; Mitsui "Ultzex" 2020L, 3010F and 3021F; Nippon NUCG-5651and Union Carbide DFDA-7540, which are all believed to be essentiallyLLDPE's, but equally MDPE, HDPE, ULDPE and LDPE can also be used to formplastic tubes in a satisfactory manner. Blends of these polyolefins arealso considered useful, especially LLDPE with HDPE due to their closecompatibility which is believed to arise from cocrystallisation.Ethylene/propylene copolymers such as EXXELOR™ PE 808 (Exxon ChemicalsLtd.) and polypropylenes such as PROPATHENE™ (ICI) are also useful forthe present purpose. Likewise, copolymers of these polyolefins withsubstituted olefins is possible.

Due to variations in commercially available bulk polymers some initialexperimentation and minor variation of the extrusion process may berequired but such is believed to be within the ordinary skill of thosein the art. Apart from the above olefinic polymers which are favored interms of availability, cost, processability and physical properties,when extruded to form a shock tube, other draw-orientablemelt-extrudable polymers of sufficient toughness and possessing adequatewater and oil resistance may be used e.g. polyesters such aspolyethylene/butyleneterephthalate (PBT) or nylons may also be used as abasis for the structural polymer matrix of the tube with similarresults. Kodar™ is a suitable polyester obtainable from EastmanChemicals. The diversity of polymers available in the plasticsextrusion-moulding field and synthetic fibre field is now so vast thatit is impossible to test them all but the expertise available in thosefields will permit an informed exploration of other polymers should thatbe desired.

The polymer that provides the bulk matrix of the tube is simply requiredto provide a tough tube of the desired dimensions and physicalproperties and to be an adequate carrier for the incorporated materialthat serves to impart powder adherent/retentive properties to the innertube surface. It needs, of course, to be melt extrudable in a mannerallowing effective powder introduction and therefore to possess, or begiven, adequate melt strength. Many of the preferred bulk polymers, e.g.LLDPEs, are melt-thinning under shear and therefore require eitherhighly skilled extrusion expertise or, if a more forgiving polymer meltis desired, a sufficient but small proportion of melt blended misciblemelt strength additive as described further below.

The basic and surprising discovery from which the present invention isderived is that for a practical shock wave conductor tube a bulk powderadherent homopolymer is not needed contrary to the long standing beliefand practice of the art. A blend in which there is separation offunction can work as well or better and be economically advantageous.

The particulate reactive material required for sustaining a shock wavewithin the tube requires the surface presence of an additive whichaccording to the present invention may be in the form of anotherpolymer, or a lower molecular weight material, which is sufficientlymiscible or compatible as to be incorporated in the bulk polymer matrixto provide an extruded tube exhibiting the desired retentive properties.The additive must not be excessively binding nor exhibit aggressive tackor rely solely on transient electrostatic properties since the reactivematerial would then be incapable of propagating the shock wave either bybeing permanently attached to the tube surface or through migration fromthe surface over a period of storage. Thus we have found that selectedmaterials should be added to the matrix polymer prior to extrusion toprovide an extrudable blend capable of being drawn to form asatisfactory tube for use as a shock wave conductor. These arecharacterized by having pendant or free functional or polar groups e.g.carboxyl, anhydride, hydroxyl, halogen, cyano, amido, sulphonate etc.,by having an inherent adherent property or by being of relatively smallmolecular size. Such materials can be selected from ethylene/acrylicacid (EAA) copolymers, ethylene/methacrylic acid (EMA) copolymers,polyisobutylenes (PIB), polybutadienes (PBD), polyethylene waxes (PEWax), ionomers, polyethylene glycols (PEG), poly-propylene glycols(PPG), ethylene vinyl alcohol resins (EVAL), buryl rubber, Rosin,maleinised polypropylene, polyacrylamide or polyacryl-amide oximeresins, polyethylene imine, sulphone or phosphonate resins. Preferablythe additive is an ethylene acrylic acid copolymer (EAA) or methacrylicacid copolymer (EMA), or an ionomer. Polymers suitable for this purposeinclude those commercially available under the Trade Marks "Primacor"(EAA), e.g. 1430, "Surlyn" 1855 (believed to be wholly or partiallyneutralized polymers of methyl acrylic acid and ethylene monomer) or8940 (Na ionomer), "Nucrel" (EMA) 403 or 410, Hyvis 30 (PIB, BPChemicals), Lithene N4 6000 (PBD, Doverstrand Ltd), Soarnol D (EVALresin, British Trades & Shippers), Portugese WW Gum Rosin from Mead KingRobinson Co Ltd, PEG 4000 (Lanster Chemicals) and lower molecular weightmaterials such as PE wax (AC 617A NE 3569, Allied Chemicals) are alsoeffective.

The terms "miscible" and more especially "compatible" should not beunderstood in any narrow sense of being free of all tendency (in Theabsence of other forces) to separate or segregate. Thus ionomers such asthose sold under the Trade Mark "Surlyn" are not considered misciblewith LLDPEs, nor are they promoted as being compatible with LLDPEs.However we have shown that under the high stress mixing and shearingforces experienced in a screw extruder they can be finely andhomogeneously dispersed to levels of say 10% w/w and any inherenttendency to segregate or for droplets to coalesce into large globulesdoes not adversely manifest itself in the short duration of extrusionprior to consolidation of the tube.

The polyethylene-miscible or compatible resin which imparts meltstrength to the polymer blend can be, for example, ethylene/vinylacetate copolymer such as CIL 605-V or ethylene/methyl acrylate orethylene/butyl acrylate (EMA or EBA esters) or a low densitypolyethylene having a melt index of 3 or less. Lupolen 2910 M is asuitable EBA ester obtainable from BASF (UK) Ltd.

Of course these polymers may include typical additives such as flameretardants antioxidants fillers, slip and anti-blocking agents, couplingagents, U.V. stabilizers, thickeners and pigments as required.

BRIEF DESCRIPTION OF DRAWINGS

A better understanding of the details of the invention will be obtainedfrom the following description and the accompanying drawings in which:

FIG. 1 is a transverse cross-section, not to scale, of the shock waveconductor of the invention; and

FIG. 2 is a flow diagram illustrating the manufacturing steps employedin the method of the invention.

Referring to FIG. 1, a cross-section of the shock wave conductor of theinvention is shown wherein 1 is the tubing wall which comprises one ofthe heretofore described plastic blends and 2 is a thinly distributeddeposit of reactive or energetic material.

Referring to FIG. 2, the steps involved in the method of manufacture ofThe shock wave conductor of FIG. 1 are illustrated. Plastic resinstorage hoppers P1, P2 and P3 contain, respectively, particulatepolyolefin resin, optional particulate resin which imparts melt strengthand particulate resin which enhances powder retention. The resins fromP1, P2 and P3 are proportioned into resin blender 10 and the blendedresin is transferred to extrusion apparatus 11. Extrusion apparatus 11produces a continuous, thick-walled primary tube having an initial innerand outer diameter greater than that desired in the final tube product.As the thick-walled tube is produced, an energetic reactive material,for example, a powdered mixture of HMX and aluminium from reservoir 12,is distributed by known means on the inner surface of the tube at a coreload of about 2-3 times that of the desired final tube product. Theextruded thick-walled, energetic material-containing tube is thendirected, as melt drawdown takes place, to a cooled, size-determiningdie 13 from which it emerges as a reduced diameter tube. After Thedrawdown size reduction, the tube is passed through a spray cooler 15and, then, to an elongation/stretching station 16. Stretching station 16preferably comprises a pair of capstans, the downstream, fast-movingcapstan rotating 5 to 6 times more rapidly than the upstream slow-movingcapstan in order to provide a corresponding elongation of the tube, andto eliminate bumpy areas and increase tensile strength. Heat fromheating unit 14 may optionally be required. After stretching at station16, optional cooling is provided at cooling unit 17 and, if desired,optional stress relief (not shown) may be given and the final product iscollected at station 18.

The position and functioning of sizing die or plate 13 is in manyinstances critical to the geometry and, hence, to the performance of thefinal finished product. The final tubing dimensions may be from 2.5 mmto 3.3 mm outside diameter and about 1.3 mm inside diameter. Plate ordie 13 governs the size and shape of the product subsequently producedat stretching station 16. Any fluctuations in the tubing leaving dieplate 13 tend to be preserved through the subsequent stretch operation.Die plate 13 may comprise, for example, a metal split ring equipped forwater cooling and lubrication, a series of such rings or a vacuum sizingdevice. The large slow moving primary capstan at station 16 is importantboth to provide control of the drawdown ratio of the primary tube and toprovide sufficient surface area and drag to prevent slippage and/or"free-wheeling" during the stretching operation. The stretch ratio iscritical to the achievement of the ultimate tensile strength of theproduct while maintaining adequate size control and eliminatingexcessive stretch in the final product. The addition of reactivematerial to the large tube at station 12 is controlled so that the finaltubing core load is in the order of 10-30 mg/m. However circumstancescould call for higher loadings as is known in the art in which caseappropriate adjustments would be made.

The plastic blend, e.g. 80/10/10, preferably comprises linear lowdensity polyethylene (LLDPE) as the major component and, for example,ethylene vinyl/acetate copolymer (EVA) and ethylene/acrylic acidcopolymer as minor components. The LLDPE gives tensile strength to thefinal product, the EVA provides melt-strength in order to extrude moreeasily a uniform product and the ethylene acrylic acid copolymer impartsenhanced powder adhesion. It will be recognized by those skilled in theart that a reduced melt drawdown ratio may obviate the need for a meltstrength enhancer or may require less of it. Further, the melt-strengthrequirement and the powder adhesion capability, may, in some instances,be provided by a single resin suitably possessing both attributes e.g.selected EVAs. The addition of the ethylene/acrylic acid copolymer at10% w/w to the blend gives excellent powder adhesion to the tubing, andlevels well in excess of 4.3 g of powder per square meter of inner tubearea are readily achievable.

The tensile strength of the shock tube of the invention is high comparedwith any known prior art shock tube. Tubing of 3.0 mm O.D. and 1.3 mmI.D. requires a load of between 90 kg and 100 kg to break it at about100% elongation. This translates to a tensile strength of 150 to 170N/mm² (20,000 to 25,000 psi). Stress-relieving will reduce tensilestrength and increase elongation to break.

It will be understood that, during the manufacturing process, variousquality control testing and inspections are performed to ensure that thecore load of reactive material is within the specified range and thatthe dimensions of the tube are uniform and within narrow limits.

The invention will now be further described by way of the followingnon-limitative Examples. Example 1 is a comparative Example not inaccordance with the invention.

EXAMPLE I

A blend of LLDPE (85%) and low functionality (2%) EVA (15%) was extrudedby a Battenfelder extruder (5.0 cm diameter, 24:1 1/d metering screw),through a 3.0 cm outer die and a 1.4 cm inner mandrel. The melt wassubjected to a 15:1 drawdown over 25 cm through a 7.6 mm diameter sizingdie and processed as shown in FIG. 2. The optional heating and coolingwere not used. The large tube dimensions were about 7.6 mm O.D. extrudedat a rate of about 5 m per minute.

After stretching, the tube size was about 3 mm O.D. and produced at arate of 45 m per minute. Explosive powder (HMX/A1) was added to thelarge tube at a rate sufficient to give a final core load of about 20mg/m (4.4 g/m² of internal area). The tensile strength of this tube wasabout 140 N/m². A break load of 80 kg was required at an extension of160%. Oil resistance was somewhat better than that of regularly producedmono-plastic shock tubing. Powder adhesion was, however, very poor aftervibration and handling of the tubing

EXAMPLE II

A blend of LLDPE (80%), EVA (10%) and EAA (10%) was extruded, cooled andstretched as described in Example 1. The tensile strength of this tubewas 170 N/m². A break load of 100 kg was required over an extension of130%. Oil resistance was unchanged from Example 1. Powder adhesion wasover 4.4 g/m² and approached 7 g/m².

EXAMPLE III

A portion of the tubing of Example II was stretched by applying theoptional heating and cooling stages. No essential differences in tubingproperties were observed.

EXAMPLE IV

A blend of LLDPE (67%), EVA (16.5%) and EAA (16.5%) was extruded underthe same conditions as Example I. All physical properties weremaintained except elongation which was about 100%.

EXAMPLE V

A blend of 80% Dowellex 2045-A, MFI 1.0, density 0.920 g/cc, (anoctene-based LLDPE); 10% CIL-605-V, MFI 0.15, density 0.923 g/cc (an EVAcopolymer containing 2% VA); and 10% Dow Primacor 1430, MFI 5.0, density0.938 g/co, (EAA copolymer containing 9% acrylic acid), i.e. an 80/10/10blend of LLPDE/EVA/EAA, produced a very useful plastics compositionwhich was extruded into tubing. Likewise 90/8/2, 90/10/0, 90/0/10 (nosizing dies), 66/17/17 and 85/15/0 compositions were produced and formedinto tubes. The extrusion temperature profile ranged from about 150° C.to 190°. Melt draw down ratios were 14:1 or less. An extrusion die ofapproximately 30 mm with a mandrel die of about 14 mm was used.Appropriate sizing dies improved uniformity of tube size. The averagecoreload of reactive material was about 22 mg.m⁻¹. The extruded tube wascold-drawn using a second capstan rotating at around 5-6 times thesurface speed of the feed capstan such that the localised draw point orneck was at the point of departure from the feed capstan. Terminal linespeed was 40-45 m/min. The true cold draw ratio of the tube was about 4(weight ratio of equal lengths of undrawn and drawn tube).

Tubing according to the invention (80/10/10) was subjected to varioustests to determine its capability in the field. Properties of Thissingle-wall (S/W) composition, O.D. 3.4 mm, I.D. 1.32 mm, are given inTable I below and compared with the currently commercially availableover-extruded NONEL tube (O/E). The tests included oil immersion, hoopstrength, sunshine exposure, shrinkage and propagation under crimp,powder migration and pull out tests.

                  TABLE I    ______________________________________    Property      O/E NONEL     S/W    Oil Resistance                  15-23 days    15 days    Hoop Strength (psi)    (Radial Burst)    25° C. 1400          1500    40° C. 1100          1250    65° C.  500           925    Sunshine Exposure                   42             7    for two days (32° C.)    then fired:-    bursts/100 meters    Crimp Shrinkage    80° C. for 1 hour    Linear (%)    8.5           1-3    Crimp 5.4 mm  0.8 to 0.5 mm 0.9 to 0.8 mm    Firings after 5/5 fail      0/5 fail    85° C. for 2 hours    Abrasion      30 turns      71 turns    Notch Test    7 kg at 60%   17 kg at 230%    Powder Migration                  5% from 18 mg/m                                5% from 18 mg/m    Pull through 5.4 mm                  9.2 kg at 340%                                14.7 at 66%    detonator crimp    (load, elongation)    ______________________________________

EXAMPLE VI

Two compositions were made as before using Dowellex 2045A LLDPE andPrimacor EAA, one containing EVA (80/10/10) and one without (43/0/10).The former was extruded at a high temperature profile (greater than 190°C.) whilst the latter was extruded at a lower temperature profile (lessthan 190° C.) at a draw down ratio of 6:1 to give tubing having theproperties indicated in Table II.

                  TABLE II    ______________________________________    Composition     80/10/10     90/0/10    Tube Size: O.D.     3.00 to 3.07 mm                                     3.00 to 3.07 mm               I.D.     1.37 mm      1.35 mm    Plastic Weight  5.26 g/m     5.26 g/m    Coreload        18.2 mg/m    18.7 mg/m    Powder Migration                    5.4%         6.9%    Hoop Strength   1620 psi     1540 psi    Abrasion Resistance                    60 turns     60 turns    Shrinkage: 1 hr 80° C.                    3.5%         3.3%    Tensile Strength:    Breakload       33.8 kg      34.9 kg    Elongation      380%         390%    Perforations/100 m                    295*         154*    Black background,    3.5 hr, air temp.    32° C., bright sunshine    ______________________________________     *NB: Commercially available NONEL yields 470 holes under the same     conditions

Thus it is apparent that a melt strength additive (EVA) may be dispensedwith by appropriate control of the extrusion conditions.

The effect of varying melt conditions while retaining the presence ofEVA (CIL 605-V) in a similar 80/10/10 blend (2045-A/605-V/1430), drawndown at 14:1, with a terminal line speed of 40-45 m/min was investigatedand the results are shown in the following Table III

                  TABLE III    ______________________________________    Sample          1        2       3     4    ______________________________________    Melt Temp (°C.)                    190      177     168   160    Coreload (mg/m) 18       19.6    19    20.6    Powder Migration (%)                    3        3.2     3.1   1.1    Shrinkage:      3        3.5     3.4   3.6    1 hr 80°C. (%)    Hoop Strength (psi)                    1550     1400    1475  1475    Breakload (kg)  35       31      30    31    Elongation (%)  460      490     460   460    Tensile Strength                    63       52      54    53    (N/mm.sup.2)    Diameter Control                    Good     Poor    Poor  Poor    ______________________________________

In the following Examples listed in Table IV a variety of compositionsof this invention based mostly on olefinic polymers (matrix) aredescribed and these are respectively: Example VII Dowellex 2045-A;Example VIII Esso 3121.73; Example IX Dow ULDPE-4001; Example XAecithene LF 3020P; Example XI Dow 2049 LLDPE; Example XII Dow 2075LLDPE; Example XIII Du Pont 12J1, (all 80%), Example XIV Dowellex 2045-A(90%). Examples VII-XIV contain Primacot 1430 (EAA) (10%) as reactivematerial adhesion enhancer and all but XIV contain CIL 605-V (EVA) (10%)as melt strength enhancer. Example XV uses CIL 605-V as matrix polymer(90%) with Primacor 1430 (10%) as adhesion promoter whilst XVI uses DuPont 29-08 HDPE (50%), CIL 605-V (40%) and Primacor 1430 (10%). Allthese compositions were made at a melt draw down ratio of 8:1 and fromthis Table it can be recognised that a variety of polymers hithertothought to be unsuitable for use in shock wave conductors can be made towork as blends.

                  TABLE IV    ______________________________________    Example      VII     VIII    IX    X     XI    ______________________________________    Tube Size:    O.D. (mm)    3       3       3.1   3.1   2.8    I.D. (mm)    1.3     1.4     1.4   1.4   1.2    Hoop         1550    1310    1200  1350  1745    Strength (psi)    Abrasion     42      46      28    43    50    Resistance (turns)    Shrinkage    2.7     2.3     5.1   4.1   2.2    1 hr 80° C. (%)    Tensile      63      64      44    53    74    Strength (N/mm.sup.2)    Breakload (kg)                 35      35      27    32    36    Elongation (%)                 460     500     500   590   370    ______________________________________    Example      XII     XIII    XIV   XV    XVI    ______________________________________    Tube Size:    O.D. (mm)    3       2.8     2.9   3.1   N/A    I.D. (mm)    1.3     1.3     1.2   1.4   N/A    Hoop         1560    1560    1550  1180  N/A    Strength (psi)    Abrasion     40      46      47    31    N/A    Resistance (turns)    Shrinkage    3.4     2.6     3.6   4.6   N/A    1 hr 80° C. (%)    Tensile      61      67      64    47    N/A    Strength (N/mm.sup.2)    Breakload (kg)                 34      33      34    28    N/A    Elongation (%)                 440     420     450   280   N/A    ______________________________________     N/A = data not available

Further tests were carried out using Aecithene LLDPE's, LF3020, MFI 1.0,density 918; LC3081, MFI 0.6, density 920; and LF3100 MFI 0.5, density918, in comparison with the Dowellex 2045-A mentioned above and theresults are indicated in the following Table V. The extrusion was run at65 rpm and the line speed was 13.2 m/min. The temperature of extrusionwas changed from high profile melt temperature i.e. about 210° C. to lowprofile melt temperature i.e about 190° C. As in previous examples blendcomposition is indicated as % matrix polymer/% melt strength enhancer(605-V)/% adhesion enhancer (1430) i.e. in these examples 80/10/10 shownas A or 90/0/10 as B. The melt draw down ratio was either 6:1 or 17:1 asindicated.

                  TABLE V    ______________________________________    Example    XV11     XVIII    IXX    XX   XXI    ______________________________________    Matrix     2045-A   2045-A   3020   3020 3020    Blend      A        B        A      B    A    Profile    High     Low      Low    Low  High    ddr        6:1      6:1      6:1    6:1  6:1    Tube Size:    O.D. (mm)  3        3        3      3    3    I.D. (mm)  1.3      1.3      1.3    1.4  1.3    Plastic (g/m)               5.26     5.26     5.2    5.3  5.2    Coreload (mg/m)               18.2     18.7     17.8   13.6 None    Migration (%)               5.4      6.9      7.5    0    --    Hoop       1620     1540     1500   1420 1485    Strength (psi)    Abrasion   60       60       53     62   56    Resistance (turns)    Shrinkage  3.5      3.3      5.5    5.8  5.8    1 hr 80° C. (%)    Tensile    33.8     34.9     N/A    36.1 34.7    Breakload (kg)    Elongation (%)               380      390      N/A    560  580    ______________________________________    Example       XXII     XXIII    XXIV   XXV    ______________________________________    Matrix        3081     3100     3020   3100    Blend         A        A        B      B    Profile       Low      High     High   High    ddr           6:1      6:1      17:1   17:1    Tube Size:    O.D. (mm)     3        3        3      3    I.D. (mm)     1.3      1.4      1.3    1.3    Plastic (g/m) 4.8      5.7      5.3    5.3    Coreload (mg/m)                  None     None     15.2   16.6    Migration (%) --       --       2.75   2.6    Hoop          1390     1400     1490   1405    Strength (psi)    Abrasion      32       59       62     63    Resistance (turns)    Shrinkage     4.6      5.1      5.2    5.86    1 hr 80° C. (%)    Tensile       33.1     34.1     32.2   28.5    Breakload (kg)    Elongation (%)                  295      570      641    500    ______________________________________

In the following Table VI the physical properties of additional examplesof shock wave conductors made in accordance with the present inventionare described. The compositions were all based on 80% Dowellex LLDPE2045-A and 10% CI L EVA 605-V with 10% of a reactive particle adherencepromoting material selected from commercially available ionomer resins,i.e. neutralised ethylene/methacrylic acid (Surlyn or Nucrel) orethylene/acrylic acid (Primacor) resins.

                  TABLE VI    ______________________________________    Example     XXVI    XXVII     XXVIII IXXX    ______________________________________    Components (%):    LLDPE 2045-A                80      80        80     80    EVA CIL 605-V                10      10        10     10    Surlyn 1855 10      --        --     --    Nucrel 403  --      --        --     10    Nucrel 410  --      --        10     --    Primacor    --      10        --     --    Tube Size:    O.D. (mm)   3.1     3.0       3.1    3.0    I.D. (mm)   1.4     1.3       1.4    1.3    Plastic (g/m)                5.5     5.2       5.3    5.2    Coreload (mg/m)                18.9    17.9      18.6   16.9    Migration (%)                4.5     9.3       12.8   1.6    Shrinkage   2.2     2.6       2.3    2.3    1 hr 80° C. (%)    Tensile     43      48        48     51    Strength (N/mm.sup.2)    Breakload (kg)                26.8    27.2      29.3   29.2    Elongation (%)                690     520       520    510    ______________________________________

The above results are quite favourable and in particular the results ofExample IXXX show Nucrel 403 (EMA) to be especially good in minimisingpowder migration.

Further work was carried out using different matrix polymers in place ofthe LLDPEs illustrated in the foregoing Examples with EVAs and EAAs asreferred to above. Satisfactory tubes were drawn at elevatedtemperatures using polypropylene based (80/10/10) compositions. Similarresults were obtained using polyester based (90/10 and 80/10/10)compositions.

EXAMPLE XXX

A polypropylene based tube composed of 80% rubber toughenedpolypropylene (90% SHELL GET6100N polypropylene with 10% EXXELOR PE 808ethylene/propylene copolymer) 10% EVA and 10% EAA (PRIMACOR) wasextruded and cold drawn at a temperature of 150° C. (achieved in afluidised bed of glass spheres). The primary tube had an externalinitial diameter of 6.3 mm and the drawn tube, at the localised drawpoint, had an external final diameter of 2.7 mm. The tube quality wasgood and powder adhesion was satisfactory.

A laboratory powder adhesion test using an LLDPE matrix polymer with astandardized reactive material was used to evaluate a variety of powderadhesion enhancing materials and the results are reported in Table VIIbelow

                  TABLE VII    ______________________________________    Powder adhesion enhancing material                         (%)    Coverage (g/m.sup.2)    ______________________________________    EAA (Primacor)       10     3.5-4    Polyisobutylene (Hyvis 30)                         1      2    Polyisobutylene (Hyvis 30)                         2      3.5    Polyisobutylene (Hyvis 30)                         5        9-9.5    Polybutadiene (Lithene N4 6000)                         3      5    Polyethylene Wax (AC617A)                         5      2    Polyethylene Wax (AC617A)                         10     3    EVAL (SOARNOL D)     2      2    EVAL (SOARNOL D)     5      5.9    Portugese WW Gum Rosin                         1      2.5-3    ______________________________________

In the following Examples higher functionality (9% VA) EVA obtainableunder the trade mark EVATANE was substituted for the EVA (lower VA) usedin earlier Examples with a view to determining the effect on surfacecoverage after loading with a standardized powder. The results areindicated in Table VIII below and it can be seen that compositions Bcontaining slightly higher functionality EVA than those of compositionsA leads to improved surface coverage but it should be appreciated thatsignificantly higher VA functionality levels could require adjustment ofthe extrusion conditions. However it is interesting to note that use ofincreased quantities of EVATANE does not have any marked effect onsurface coverage. This also shows that certain EVAs can function asadhesion promoters in the bulk polymer matrix.

                  TABLE VIII    ______________________________________    POLYMER    BLEND COMPOSITION %                     SURFACE COVERAGE g.m.sup.-2    ______________________________________    LLDPE : Lower VA EVA    A1 90:10         1.88    A2 90:10         1.09    A3 90:10         1.09    LLDPE : Higher VA EVA    B1 90:10         2.31    B2 30:20         2.33    B3 60:40         2.74    ______________________________________

We claim:
 1. A cold drawn low energy shock wave conductor comprising anextruded single-wall, dimensionally stable plastic tube having an innersurface coated with a particulate reactive energetic material, theplastic of the tube comprising a homogeneous extrudable blend of a majoramount of a draw orientable polymer resin lacking adequate reactivematerial-retaining properties, and a minor amount of a modifier which isa miscible or compatible material which imparts an enhanced reactivematerial-retaining capability to the inner surface of said extrudedplastic tube.
 2. A shock wave conductor according to claim 1 whereinsaid polymer resin is in the form of a continuous matrix and themodifier is distributed in the matrix polymer such that it has a greaterconcentration at said inner surface of the tube than in the body of thematrix.
 3. A shock wave conductor according to claim 2 wherein saidmodifier is present as non-contiguous particles or fibrils within thematrix.
 4. A shock wave conductor according to claim 3 wherein saidparticles are about 0.5μ in size.
 5. A shock wave conductor according toclaim 2 wherein said modifier is concentrated in segregated zones in thematrix.
 6. A shock wave conductor according to claim 1 wherein thepolymer resin is a fibre forming a polymer.
 7. A shock wave conductoraccording to claim 1 wherein the polymer resin is selected from thegroup consisting of (1) addition polymers and condensation polymershaving a substantially linear hydrocarbon backbone structure; (2) suchpolymers wherein the backbone structure is interrupted by hetero atoms;(3) such polymers wherein the backbone structure is substituted by polarfunctional groups and such polymers wherein the backbone structure isinterrupted by hetero atoms and substituted polar functional groups. 8.A shock wave conductor according to claim 7 wherein the addition polymeris selected from the group consisting of a polyolefin homopolymer andpolyolefin copolymer.
 9. A shock wave conductor according to claim 7 or8 wherein the addition polymer is selected from the group consisting ofa copolymer of ethylene and a copolymer of an alpha-olefin with asubstituted olefin monomer.
 10. A shock wave conductor according toclaim 7 wherein the condensation polymer is selected from the groupconsisting of a polyester and a polyamide.
 11. A shock wave conductoraccording to claim 1 wherein said modifier is selected from the groupconsisting of a homo-polymer, a copolymer resin, and a material of lowermolecular weight than the homopolymer and copolymer resin but of likeproperties.
 12. A shock wave conductor according to claim 11 wherein themodifier is selected form the group consisting of ionomers,ethylene/acrylic acid (EAA) copolymers, ethylene/methacrylic acid (EMA)copolymers, polyisobutylenes (PIB), polybutadienes (PBD), polyethylenewaxes (PE Wax), polyethylene glycols (PEG), poly-propylene glycols(PPG), ethylene vinyl alcohol resins (EVAL), butyl rubber, Rosin,maleinised polypropylene, polyacrylamide or poly-acrylamide oximeresins, polyethylene imine, sulphone and phosphonate resins.
 13. A shockwave conductor according to claim 11 wherein the modifier is selectedfrom the group consisting of ethylene/acrylic acid (EAA) copolymers,ethylene/methacrylic acid (EMA) copolymers and neutralised ionomersthereof.
 14. A shock wave conductor according to claim 11 wherein themodifier is selected from the group consisting of polyisobutylenes(PIB), polybutadienes (PBD), polyethylene waxes (PE Wax), polyethyleneglycols (PEG), poly-propylene glycols (PPG), ethylene vinyl alcoholresins (EVAL), butyl rubber, Rosin, maleinised polypropylene,polyacrylamide, poly-acrylamide oxime resins, polyethylene imine,sulphone and phosphonate resins.
 15. A shock wave conductor according toclaim 11 wherein the modifier is selected from the group consisting ofethylene/acrylic acid (EAA) copolymers, ethylene/methacrylic acids (EMA)copolymers and partially and wholly neutralized monomers thereof.
 16. Ashock wave conductor according to claim 1 comprising a minor amount of ahomopolymer or copolymer resin or cross-linking agent which is misciblein or compatible with said orientable polymer resin and which impartsmelt strength and aids in tube extrusion.
 17. A shock wave conductoraccording to claim 16 wherein the melt strength/extrusion improvingresin is selected from the group consisting of ethylene/vinyl acetatecopolymers and copolymers of ethylene with lower alkyl esters of acrylicor methacrylic acid.
 18. A shock wave tube according to claim 1 having atensile strength of up to 170 newtons per square millimeter.
 19. A shockwave conductor according to claim 1 wherein the coreload is from about15 to 60 mg.m⁻¹.
 20. A shock wave conductor according to claim 1 whereinthe coreload is up to about 20 mg.m⁻¹.
 21. A shock wave conductoraccording to claim 1 wherein the tube has dimensions of from 2.5 to 3.3mm O.D. and about 1.3 mm I.D.
 22. A shock wave conductor according toclaim 1 wherein the tube is treated externally with agents to improveresistance to water or oil or to water and oil.
 23. A shock waveconductor according to claim 1 wherein the polymer resin is acondensation polymer having a substantially linear hydrocarbon backbonestructure interrupted by hetero atoms.
 24. A shock wave conductoraccording to claim 9 or claim 23 wherein the polymer resin has asubstantially linear hydrocarbon backbone structure substituted by polarfunctional groups.
 25. A low energy shock wave conductor in the form ofa cold drawn extruded single wall, dimensionally stable plastic tubehaving an inner surface coated with particulate reactive energeticmaterial formed according to the method which comprises(a) extruding apolymeric melt through a wide annular die in the form of a thick walledtube while distributing particulate reactive energetic material in acore load per unit of length on the inner surface of the thick walledtube, the polymeric melt comprising a substantially homogenous blend ofa major amount of a draw orientable melt-extrudable polymer resin and aminor amount of a miscible or compatible material as an adhesionpromoting agent which is distributed in the extruded melt such that ithas a greater concentration at the inner surface of the tube than in thebody of the extruded melt and imparts an enhanced reactive energeticmaterial-retaining capability to the inner surface of the extruded tube,and (b) cold drawing the thick walled tube to elongate and form alocalized drawing point to increase tube tensile strength, reduce wallthickness, and to reduce core load per unit length of the reactiveenergetic material.
 26. A low energy shock wave conductor according toclaim 25 in the form of a cold drawn extruded single wall, dimensionallystable plastic tube having an inner surface coated with a particulatereactive energetic material wherein the polymer melt further comprises aminor amount of a homopolymer or copolymer resin which is miscible inthe polymer melt and which imparts melt strength and aids in tubeextrusion.
 27. A low energy shock wave conductor comprising a colddrawn, dimensionally stable tube made of extrudable plastics material,and containing a core loading of a particulate reactive energeticmaterial, wherein the said tube has an extruded single-wall, andthroughout its length an inner surface circumscribing a void throughwhich a shock wave may be transmitted, the said surface retaining saidparticulate reactive energetic material as a layer thereon, and the saidplastics material comprises a substantially homogeneous blend of a majoramount of a draw orientable polymer resin lacking adequate reactivematerial-retaining properties, and a minor amount of a modifier which isa miscible or compatible material which imparts an enhanced reactivematerial-retaining capability to said polymer resin.
 28. A low energyshock wave conductor comprising an extruded single-wall, dimensionallystable plastic tube having an inner surface coated with a particulatereactive energetic material, the plastic of the tube comprising ahomogeneous extrudable blend of a major amount of a draw orientablepolymer resin lacking adequate reactive material-retaining properties,and a minor amount of a modifier which is a miscible or compatiblematerial which imparts an enhanced reactive material-retainingcapability to the inner surface of said extruded plastic tube whereinthe polymer resin is a continuous matrix and the modifier is present asfibrils a few microns in length with aspect ratios of from about 6 toabout 10 aligned with the tube axis and distributed in the matrixpolymer such that it has a greater concentration at the inner surface ofthe tube than in the body of the matrix.
 29. A cold drawn shock waveconductor according to claim 28.